| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:78867471-78867621 | Rare:73 | ||||
| chr6:79078135-79078613 | Common:1; Rare:199 | ||||
| chr6:79234554-79235043 | Common:4; Rare:104 | ||||
| chr6:79537351-79537665 | Common:2; Rare:98; Clinvar:4 | ||||
| chr6:79631156-79631358 | Common:2; Rare:51 | ||||
| chr6:79947536-79947724 | Common:1; Rare:77; Clinvar:5; Clinvar (benign):1 | ||||
| chr6:82247711-82247821 | Rare:36 | ||||
| chr6:83193201-83193397 | Common:3; Rare:68 | ||||
| chr6:83708763-83708975 | Common:3; Rare:62 | ||||
| chr6:83853507-83853650 | Common:1; Rare:42 | ||||
| chr6:85593796-85593927 | Rare:48 | ||||
| chr6:85643817-85643931 | Common:2; Rare:36 | ||||
| chr6:87155229-87155666 | Rare:134 | ||||
| chr6:87589940-87590169 | Common:3; Rare:109; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr6:87702189-87702514 | Common:2; Rare:102 |